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Immunohistochemistry Tissue sections were dewaxed and hydrated followed by high temperature antigen repair, followed by endogenous occlusion using 3% H 2 O 2 (88597, Merck, USA) and exogenous occlusion using 5% BSA (V900933, Sigma, USA), and at the end of the occlusion dropwise addition of diluted antibodies (ATP5D, 1:250, ab97491, Abcam, UK